Discovery of a Unique Novel Clade of Mosquito-Associated Bunyaviruses

Author:

Marklewitz Marco1,Zirkel Florian1,Rwego Innocent B.234,Heidemann Hanna1,Trippner Pascal1,Kurth Andreas5,Kallies René1,Briese Thomas6,Lipkin W. Ian6,Drosten Christian1,Gillespie Thomas R.23,Junglen Sandra1

Affiliation:

1. Institute of Virology, University of Bonn Medical Centre, Bonn, Germany

2. Department of Environmental Studies and Program in Population Biology, Ecology and Evolution, Emory University, Atlanta, Georgia, USA

3. Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA

4. College of Natural Sciences, Makerere University, Kampala, Uganda

5. Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany

6. Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, New York, USA

Abstract

ABSTRACT Bunyaviruses are the largest known family of RNA viruses, infecting vertebrates, insects, and plants. Here we isolated three novel bunyaviruses from mosquitoes sampled in Côte d'Ivoire, Ghana, and Uganda. The viruses define a highly diversified monophyletic sister clade to all members of the genus Orthobunyavirus and are virtually equidistant to orthobunyaviruses and tospoviruses. Maximal amino acid identities between homologous putative proteins of the novel group and orthobunyaviruses ranged between 12 and 25%. The type isolates, tentatively named Herbert virus (HEBV), Taï virus (TAIV), and Kibale virus (KIBV), comprised genomes with L, M, and S segments of about 7.4 kb, 2.7 kb, and 1.1 kb, respectively. HEBV, TAIV, and KIBV encode the shortest bunyavirus M segments known and did not seem to encode NSs and NSm proteins but contained an elongated L segment with an ∼500-nucleotide (nt) insertion that shows no identity to other bunyaviruses. The viruses replicated to high titers in insect cells but did not replicate in vertebrate cells. The enveloped virions were 90 to 110 nm in diameter and budded at cellular membranes with morphological features typical of the Golgi complex. Viral RNA recovered from infected cells showed 5′-terminal nontemplated sequences of 9 to 22 nt, suggestive of cap snatching during mRNA synthesis, as described for other bunyaviruses. Northern blotting identified RNA species of full and reduced lengths, suggested upon analogy with other bunyaviruses to constitute antigenomic-sense cRNA and transcript mRNAs, respectively. Functional studies will be necessary to determine if this group of viruses constitutes a novel genus in the bunyavirus family.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference106 articles.

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